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Study Coordinator

The Study Coordinator has overall responsibility for oversight of day to day activities during the course of the study through active coordination of all involved functions.  These positions will focus primarily on Toxicology studies.

Study Coordinator

  • Coordinate client study activities based on study protocols and according to regulatory guidelines
  • Assists Study Directors in designing, conducting and reporting preclinical studies
  • Assists Study Director with QA audit responses
  • Ability to conduct a broad range of study procedures without supervision and the ability to troubleshoot experimental problems when necessary
  • Continually work to adapt and improve systems (e.g. experimental data collection, study conduct etc.) to make them more efficient and effective
  • Draft deviation and protocol amendments
  • QC study protocols and/or reports
  • Prepare raw data notebooks and pertinent records, and ensure these records are in compliance with applicable federal guidelines

Requirements:

  • Prefer at least 2 years’ experience as a lab tech in a CRO environment (in vivo)
  • Minimum of a BA or equivalent years of experience
  • High degree of technical proficiency
  • High level of attention to detail and familiarity with variety of study types
  • Working knowledge of Provantis
  • Ability to work efficiently under tight time constraints and as a member of a team
  • Strong written work            
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